grade
technical grade
Quality Level
assay
90%
refractive index
n20/D 1.485 (lit.)
bp
128 °C/3 mmHg (lit.)
mp
50 °C (lit.)
density
1.066 g/mL at 25 °C (lit.)
functional group
amide, amine
SMILES string
CC(=O)NCCN
InChI
1S/C4H10N2O/c1-4(7)6-3-2-5/h2-3,5H2,1H3,(H,6,7)
InChI key
DAKZISABEDGGSV-UHFFFAOYSA-N
General description
N-(2-Aminoethyl)acetamide is an organic building block.
Application
N-(2-Aminoethyl)acetamide may be used in the preparation of mixed two-component monolayers on glassy carbon. It may be used in the synthesis of lysidine.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
>230.0 °F - closed cup
flash_point_c
> 110 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
The Mechanism of Acid Hydrolysis of Lysidine and N-(2-Aminotheyl) acetamide and Related Amides.
Haake P and Watson J.
The Journal of Organic Chemistry, 35(12), 4063-4067 (1970)
Yoonkyung Kim et al.
Purinergic signalling, 5(1), 39-50 (2008-07-05)
As a continued effort to develop multivalent ligands to enhance the pharmacological effects of monomeric drugs, DITC-APEC, a chemically reactive nucleoside A(2A) adenosine receptor (AR) agonist, was employed to derivatize the surface of third-generation (G3) polyamidoamine (PAMAM) dendrimers. The resulting
Emma J Wright et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 20(19), 5550-5554 (2014-04-12)
Mixed two-component monolayers on glassy carbon are prepared by electrochemical oxidation of N-(2-aminoethyl)acetamide and mono-N-Boc-hexamethylenediamine in mixed solution. Subsequent N-deprotection, amide coupling and solid-phase synthetic steps lead to electrode-surface functionalisation with maleimide, with controlled partial coverage of this cysteine-binding group
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 397261-25G | 04061836826789 |
| 397261-5G | 04061836820497 |